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  • 152784-11-7 Structure
  • Basic information

    1. Product Name: WILD 20
    2. Synonyms: WILD 20
    3. CAS NO:152784-11-7
    4. Molecular Formula: C53H97N3O28
    5. Molecular Weight: 1224.34058
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 152784-11-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 1343.8°Cat760mmHg
    3. Flash Point: 766.5°C
    4. Appearance: /
    5. Density: 1.49g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.628
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: WILD 20(CAS DataBase Reference)
    11. NIST Chemistry Reference: WILD 20(152784-11-7)
    12. EPA Substance Registry System: WILD 20(152784-11-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 152784-11-7(Hazardous Substances Data)

152784-11-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152784-11-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,7,8 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 152784-11:
(8*1)+(7*5)+(6*2)+(5*7)+(4*8)+(3*4)+(2*1)+(1*1)=137
137 % 10 = 7
So 152784-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C53H97N3O28/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-26(62)25(54)24-75-49-41(71)39(69)43(31(22-60)78-49)80-51-42(72)47(84-53(52(73)74)18-27(63)33(55)46(83-53)35(65)28(64)19-57)44(32(23-61)79-51)81-48-34(56)45(37(67)30(21-59)76-48)82-50-40(70)38(68)36(66)29(20-58)77-50/h16-17,25-51,57-72H,2-15,18-24,54-56H2,1H3,(H,73,74)/b17-16+/t25?,26?,27-,28?,29+,30+,31+,32+,33+,34+,35?,36-,37-,38-,39+,40+,41+,42+,43+,44-,45+,46+,47+,48-,49+,50-,51-,53-/m0/s1

152784-11-7Upstream product

152784-11-7Downstream Products

152784-11-7Relevant articles and documents

Preparation and characterization of four new variously deacetylated lysogangliosides, breakdown products of GM1

Cavallo, Giovanni,Iavarone, Carlo,Tubaro, Ezio

, p. 251 - 266 (2007/10/02)

Four new deacetylated lysogangliosides were obtained through alkaline hydrolysis of either C18 or C20 sphingosine homologues of GM1.By this procedure, both the fatty acids residue and the N-acetyl group of sialic acid were removed to give mono-N-acetyl-lysoGM1 (C18 and C20); the additional loss of the N-acetyl group of the acetylgalactosamine moiety gave de-N-acetyl-lysoGM1 (C18 and C20) with three free amino groups.The structures of four deacetylated lysogangliosides were unambiguously characterized by chemical analysis and 1H and 13C NMR spectroscopy as well as by negative ion FABMS.The aim of this study was to isolate pure breakdown products of gangliosides, enabling the evaluation of the mechanism of action of glycosphingolipids through their cleavage and identification of structures of potential pharmacological activity.These new substances were prepared as candidates to influence eicosanoid production and the mechanisms dependent on protein kinase C and phospholipase A2.

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